Jackson Janna R, Kirby Tyler J, Fry Christopher S, Cooper Robin L, McCarthy John J, Peterson Charlotte A, Dupont-Versteegden Esther E
Department of Rehabilitation Sciences, College of Health Sciences, University of Kentucky, Lexington, KY USA ; Center for Muscle Biology, University of Kentucky, Lexington, KY USA.
Department of Physiology, College of Medicine, University of Kentucky, Lexington, KY USA ; Center for Muscle Biology, University of Kentucky, Lexington, KY USA ; Present address: Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY USA.
Skelet Muscle. 2015 Nov 16;5:41. doi: 10.1186/s13395-015-0065-3. eCollection 2015.
Satellite cells, or muscle stem cells, have been thought to be responsible for all muscle plasticity, but recent studies using genetically modified mouse models that allow for the conditional ablation of satellite cells have challenged this dogma. Results have confirmed the absolute requirement of satellite cells for muscle regeneration but surprisingly also showed that they are not required for adult muscle growth. While the function of satellite cells in muscle growth and regeneration is becoming better defined, their role in the response to aerobic activity remains largely unexplored. The purpose of the current study was to assess the involvement of satellite cells in response to aerobic exercise by evaluating the effect of satellite cell depletion on wheel running performance.
Four-month-old female Pax7/DTA mice (n = 8-12 per group) were satellite cell depleted via tamoxifen administration; at 6 months of age, mice either remained sedentary or were provided with running wheels for 8 weeks. Plantaris muscles were significantly depleted of Pax7+cells (≥90 % depleted), and 8 weeks of wheel running did not result in an increase in Pax7+ cells, or in myonuclear accretion. Interestingly, satellite cell-depleted animals ran ~27 % less distance and were 23 % slower than non-depleted animals. Wheel running was associated with elevated succinate dehydrogenase activity, muscle vascularization, lipid accumulation, and a significant shift toward more oxidative myosin heavy chain isoforms, as well as an increase in voltage dependent anion channel abundance, a marker of mitochondrial density. Importantly, these changes were independent of satellite cell content. Interestingly, depletion of Pax7+ cells from intra- as well as extrafusal muscle fibers resulted in atrophy of intrafusal fibers, thickening of muscle spindle-associated extracellular matrix, and a marked reduction of functional outcomes including grip strength, gait fluidity, and balance, which likely contributed to the impaired running performance.
Depletion of Pax7-expressing cells in muscle resulted in reduced voluntary wheel running performance, without affecting markers of aerobic adaptation; however, their absence may perturb proprioception via disruption of muscle spindle fibers resulting in loss of gross motor coordination, indicating that satellite cells have a yet unexplored role in muscle function.
卫星细胞,即肌肉干细胞,一直被认为是所有肌肉可塑性的原因,但最近使用基因改造小鼠模型进行的研究对这一教条提出了挑战,这些模型允许对卫星细胞进行条件性消融。结果证实了卫星细胞对肌肉再生的绝对需求,但令人惊讶的是,研究还表明它们并非成年肌肉生长所必需。虽然卫星细胞在肌肉生长和再生中的功能越来越明确,但其在有氧运动反应中的作用仍 largely 未被探索。本研究的目的是通过评估卫星细胞耗竭对轮转运动表现的影响,来评估卫星细胞在有氧运动反应中的参与情况。
通过给予他莫昔芬,使 4 个月大的雌性 Pax7/DTA 小鼠(每组 n = 8 - 12 只)的卫星细胞耗竭;在 6 个月大时,小鼠要么保持 sedentary,要么配备跑步轮 8 周。比目鱼肌中的 Pax7+细胞显著减少(≥90%被耗尽),并且 8 周的轮转运动并未导致 Pax7+细胞增加,也未导致肌核增加。有趣的是,卫星细胞耗竭的动物跑动的距离比未耗竭的动物少约 27%,速度慢 23%。轮转运动与琥珀酸脱氢酶活性升高、肌肉血管化、脂质积累以及向更多氧化型肌球蛋白重链异构体的显著转变相关,同时电压依赖性阴离子通道丰度增加,这是线粒体密度的一个标志物。重要的是,这些变化与卫星细胞含量无关。有趣的是,肌梭内和肌梭外肌纤维中 Pax7+细胞的耗竭导致肌梭内纤维萎缩、肌梭相关细胞外基质增厚,以及包括握力、步态流畅性和平衡在内的功能结果显著降低,这可能导致了跑步表现受损。
肌肉中表达 Pax7 的细胞耗竭导致自愿轮转运动表现降低,而不影响有氧适应的标志物;然而,它们的缺失可能通过破坏肌梭纤维扰乱本体感觉,导致总体运动协调能力丧失,表明卫星细胞在肌肉功能中具有尚未被探索的作用。